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Nitin Udar

Showing results (1-10 of 41) with videos related to

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Clinical Chemistry|February 24, 2009
A multiplex assay for detecting genetic variations in CYP2C9, VKORC1, and GGCX involved in warfarin metabolismAlex J Rai, Nitin Udar, Rana Saad, et al.
Molecular Vision|March 3, 2011
Developmental or degenerative--NR2E3 gene mutations in two patients with enhanced S cone syndromeNitin Udar, Kent Small, Meenal Chalukya, et al.
Cornea|August 6, 2009
SOD1 haplotypes in familial keratoconusNitin Udar, Shari R Atilano, Kent Small, et al.
Human Mutation|August 26, 2003
Comparative analysis of the FOXL2 gene and characterization of mutations in BPES patientsNitin Udar, Vivek Yellore, Meenal Chalukya, et al.
Plos One|January 29, 2021
Low frequency mitochondrial DNA heteroplasmy SNPs in blood, retina, and [RPE+choroid] of age-related macular degeneration subjectsShari R Atilano, Nitin Udar, Timothy A Satalich, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
New mutation, P575L, in the GUCY2D gene in a family with autosomal dominant progressive cone degenerationKent W Small, Rosamaria Silva-Garcia, Nitin Udar, et al.
American Journal of Ophthalmology|October 1, 2003
Hereditary motor and sensory neuropathy type VI with optic atrophyIrene Voo, Bryan E Allf, Nitin Udar, et al.
Cornea|January 1, 2004
Keratoconus--no association with the transforming growth factor beta-induced gene in a cohort of American patientsNitin Udar, M Cristina Kenney, Meenal Chalukya, et al.
Ophthalmology. Retina|February 13, 2022
North Carolina Macular Dystrophy: Long-term Follow-up of the Original FamilyKent W Small, Robert Wiggins, Nitin Udar, et al.
Retina (Philadelphia, Pa.)|August 25, 2022
CONGENITAL POSTERIOR POLAR CHORIORETINAL HYPOPLASIA: Expansion of the Clinical Spectrum, Mutation, and Its Association With PRDM13Kent W Small, Caroline A Tawfik, Nitin Udar, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Clinical Chemistry|February 24, 2009
A multiplex assay for detecting genetic variations in CYP2C9, VKORC1, and GGCX involved in warfarin metabolismAlex J Rai, Nitin Udar, Rana Saad, et al.
Molecular Vision|March 3, 2011
Developmental or degenerative--NR2E3 gene mutations in two patients with enhanced S cone syndromeNitin Udar, Kent Small, Meenal Chalukya, et al.
Cornea|August 6, 2009
SOD1 haplotypes in familial keratoconusNitin Udar, Shari R Atilano, Kent Small, et al.
Human Mutation|August 26, 2003
Comparative analysis of the FOXL2 gene and characterization of mutations in BPES patientsNitin Udar, Vivek Yellore, Meenal Chalukya, et al.
Plos One|January 29, 2021
Low frequency mitochondrial DNA heteroplasmy SNPs in blood, retina, and [RPE+choroid] of age-related macular degeneration subjectsShari R Atilano, Nitin Udar, Timothy A Satalich, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
New mutation, P575L, in the GUCY2D gene in a family with autosomal dominant progressive cone degenerationKent W Small, Rosamaria Silva-Garcia, Nitin Udar, et al.
American Journal of Ophthalmology|October 1, 2003
Hereditary motor and sensory neuropathy type VI with optic atrophyIrene Voo, Bryan E Allf, Nitin Udar, et al.
Cornea|January 1, 2004
Keratoconus--no association with the transforming growth factor beta-induced gene in a cohort of American patientsNitin Udar, M Cristina Kenney, Meenal Chalukya, et al.
Ophthalmology. Retina|February 13, 2022
North Carolina Macular Dystrophy: Long-term Follow-up of the Original FamilyKent W Small, Robert Wiggins, Nitin Udar, et al.
Retina (Philadelphia, Pa.)|August 25, 2022
CONGENITAL POSTERIOR POLAR CHORIORETINAL HYPOPLASIA: Expansion of the Clinical Spectrum, Mutation, and Its Association With PRDM13Kent W Small, Caroline A Tawfik, Nitin Udar, et al.
Pageof 5